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A C Papp

Showing results (21-30 of 39) with videos related to

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Clinical Pharmacology and Therapeutics|February 4, 2011
Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapyW Sadee, D Wang, A C Papp, et al.
Clinical Pharmacology and Therapeutics|September 10, 2013
Profiling solute carrier transporters in the human blood-brain barrierE G Geier, E C Chen, A Webb, et al.
Human Mutation|January 1, 1996
Nonsense mutations in a Becker muscular dystrophy and an intermediate patientT W Prior, C Bartolo, A C Papp, et al.
Human Molecular Genetics|July 1, 1994
Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16T W Prior, C Bartolo, A C Papp, et al.
American Journal of Human Genetics|July 1, 1995
Spectrum of small mutations in the dystrophin coding regionT W Prior, C Bartolo, D K Pearl, et al.
Human Mutation|January 1, 1993
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysisT W Prior, A C Papp, P J Snyder, et al.
Human Molecular Genetics|March 1, 1993
Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formationT W Prior, A C Papp, P J Snyder, et al.
Nature Genetics|August 1, 1993
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patientT W Prior, A C Papp, P J Snyder, et al.
Journal of Medical Genetics|April 1, 1996
A novel splice site mutation in a Becker muscular dystrophy patientC Bartolo, A C Papp, P J Snyder, et al.
American Journal of Medical Genetics|March 1, 1994
Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detectionT W Prior, A C Papp, P J Snyder, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Clinical Pharmacology and Therapeutics|February 4, 2011
Pharmacogenomics of the RNA world: structural RNA polymorphisms in drug therapyW Sadee, D Wang, A C Papp, et al.
Clinical Pharmacology and Therapeutics|September 10, 2013
Profiling solute carrier transporters in the human blood-brain barrierE G Geier, E C Chen, A Webb, et al.
Human Mutation|January 1, 1996
Nonsense mutations in a Becker muscular dystrophy and an intermediate patientT W Prior, C Bartolo, A C Papp, et al.
Human Molecular Genetics|July 1, 1994
Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16T W Prior, C Bartolo, A C Papp, et al.
American Journal of Human Genetics|July 1, 1995
Spectrum of small mutations in the dystrophin coding regionT W Prior, C Bartolo, D K Pearl, et al.
Human Mutation|January 1, 1993
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysisT W Prior, A C Papp, P J Snyder, et al.
Human Molecular Genetics|March 1, 1993
Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formationT W Prior, A C Papp, P J Snyder, et al.
Nature Genetics|August 1, 1993
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patientT W Prior, A C Papp, P J Snyder, et al.
Journal of Medical Genetics|April 1, 1996
A novel splice site mutation in a Becker muscular dystrophy patientC Bartolo, A C Papp, P J Snyder, et al.
American Journal of Medical Genetics|March 1, 1994
Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detectionT W Prior, A C Papp, P J Snyder, et al.
Pageof 4